K-number	K222482
Device name	AGILON XO Shoulder System
Applicant	Implantcast GmbH
Product code	KWT
Device class	Class II
Decision date	Sep 28, 2022
Decision	Substantially Equivalent
Regulation	888.3650

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Source

View the full FDA submission: accessdata.fda.gov

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AGILON XO Shoulder System

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